A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14389363



Internal ID22210984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85643001..85655200hg38UCSC Ensembl
chr16:85676607..85688806hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3812200
hg1912200
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213140
Supporting Variants
SamplesHG00732
Known GenesGSE1, MIR7851
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14389363
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer